Adamou J E, Aiyar N, Van Horn S, Elshourbagy N A
Department of Molecular Genetics, SmithKline Beecham Pharmaceuticals, King of Prussia, PA 19406, USA.
Biochem Biophys Res Commun. 1995 Apr 17;209(2):385-92. doi: 10.1006/bbrc.1995.1515.
A full-length clone encoding the human VIP-2 receptor was isolated from a human placenta cDNA library. The 1317-bp cDNA insert encodes a protein of 438 amino acids which is a member of the seven transmembrane domain G-protein-coupled receptor superfamily. Expression of the human VIP-2 receptor in COS-7 cells confered high affinity binding to [125I] VIP (IC50 = 0.93 nM), which was displaced by unlabeled PACAP-38 (IC50 = 6.2 nM). VIP and PACAP-38 were equipotent in stimulating accumulation of cAMP in COS-7 cells transfected with the human VIP-2 receptor. Northern blot analysis revealed two VIP-2 receptor mRNAs of 4.6 kb and 2.3 kb in size which were expressed predominantly in the human skeletal muscle and to a lesser extent in the human brain, heart, pancreas and placenta.
从人胎盘cDNA文库中分离出编码人VIP-2受体的全长克隆。1317bp的cDNA插入片段编码一个由438个氨基酸组成的蛋白质,该蛋白质是七跨膜结构域G蛋白偶联受体超家族的成员。人VIP-2受体在COS-7细胞中的表达赋予了对[125I]VIP的高亲和力结合(IC50 = 0.93 nM),未标记的PACAP-38可将其取代(IC50 = 6.2 nM)。VIP和PACAP-38在刺激转染了人VIP-2受体的COS-7细胞中cAMP积累方面具有同等效力。Northern印迹分析显示大小为4.6 kb和2.3 kb的两种VIP-2受体mRNA,它们主要在人骨骼肌中表达,在人脑、心脏、胰腺和胎盘中表达较少。